COVID-19 is an airway disease that also affects the nervous system.1 Therefore, neurological and neurocognitive symptoms may be a part of the postacute sequelae of SARS-CoV-2 infection (PASC) syndrome. PASC may be found to affect a high proportion of people who had mild cases of COVID-19, and there is an urgent need for a detailed description of PASC in nonhospitalized patients.2,3 This cohort study examines self-reported memory problems 8 months after COVID-19 infection.
This cohort study was approved by the Regional Research Ethics Committee according to the Declaration of Helsinki. Eligible participants provided informed consent by signing an online electronic consent form and completing an online baseline questionnaire and follow-up questionnaires. This study used the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline.
We followed a cohort of 13 001 adults who were invited after (1) having their clinical specimen analyzed for SARS-CoV-2 at 4 large accredited laboratories in Norway or (2) being randomly selected from the Norwegian population (untested). All adults who were tested for COVID between February 1 and April 15, 2020, were invited (eFigure in the Supplement). Nearly all testing in Norway during that time was on symptomatic patients and free of charge.4
We collected data on demographics, underlying medical conditions, symptoms, health-related quality of life from the RAND 36-Item Health Survey, memory problems, and known confounders for memory problems (eAppendix in the Supplement). Data from participants who were hospitalized are not reported in this study.
The main outcome was self-reported memory problems 8 months after infection, and the exposure was SARS-CoV-2 status (ie, positive, negative, or untested). To determine whether differences in the outcome between the exposure groups remained after adjusting for confounding, we applied a multiple logistic regression model that included age, gender, and known confounders for memory problems (RAND-36 items for physical health limitation, pain, feeling energetic, and mood). SPSS version 27 (IBM) and R version 4.0.3 (R Project for Statistical Computing) were used for the statistical computations. Statistical tests were 2-tailed, and the significance level was set to P < .05. Data analyses were performed on May 10 and May 13, 2021.
We sent up to 3 electronic invitations to 53 168 invitees, and after exclusions, 13 001 (24%) participants completed the baseline questionnaire and were followed up for 8 months (Table). The mean (SD) age was 47 (14.3) years, and 8642 (66%) were women.
At follow-up, a mean (SD) of 257 (32) days after baseline, 9705 of 13 001 participants (75%) responded, and 72 of 651 of the participants (11%) in the SARS-CoV-2–positive group reported memory problems. In contrast, 254 of 5712 participants (4%) in the SARS-CoV-2–negative group or 80 of 3342 participants (2%) in the untested randomly selected reported memory problems (Figure).
In the multiple logistic regression model, SARS-CoV-2 positivity at baseline was strongly associated with reporting memory problems at 8 months follow-up (odds ratio [OR], 4.66; 95% CI, 3.25-6.66) compared to the untested randomly selected group. At follow-up, 267 of 649 participants (41%) in the SARS-CoV-2–positive group reported a significant worsening of health compared with 1 year prior, and 81 of 651 participants (12%) in the SARS-CoV-2–positive group also reported problems concentrating. Additionally, 59 of 267 participants (82%) in the SARS-CoV-2–positive group who reported memory problems also reported a worsening of health. Feeling depressed, having less energy, or pain were reported relatively equally by the different groups (Table).
We examined the prevalence of self-reported memory problems in a large group of COVID-19 patients who were not hospitalized and had a relatively mild disease. Eight months after the positive SARS-CoV-2 test, the prevalence of memory problems in this group was higher than in the control group with a negative test or in the untested control population.
Most of the SARS-CoV-2–positive participants with memory problems also reported a worsening of their health compared with 1 year prior. Our findings suggest that SARS-CoV-2 may negatively impact memory even 8 months after having a mild case of the disease, and this can be associated with a worsening of health and PASC. The findings are a strong impetus to reconsider the notion that COVID-19 can be a mild disease. It also questions whether the current home-treatment strategies are optimal for the long-term outcome. Our results suggest that memory problems may be a part of PASC, but firmer conclusions should await a longer follow-up period.
This study had limitations. Although we ran multiple logistic regression that adjusted for several likely confounders, there may still have been unmeasured or residual confounding. An additional limitation of the study is that knowledge of COVID-19 status and symptoms at baseline could have led to participation bias or response bias during follow up. The low overall response rate of 24% may limit the generalizability of our findings. A strength of the study is the inclusion of 2 relevant comparison groups.
The lack of objective memory tests limits strong conclusions. However, subjective memory concerns have been shown to reflect objective problems and observable changes in everyday function even when controlling for associated factors, such as depression.5 Self-reported memory problems are also a risk factor for later mild cognitive impairment or dementia.6 Nevertheless, a more detailed examination of what type of memory problems are specific for PASC, like working memory vs long-term memory, is warranted in future studies.
Accepted for Publication: May 21, 2021.
Published: July 29, 2021. doi:10.1001/jamanetworkopen.2021.18717
Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2021 Søraas A et al. JAMA Network Open.
Corresponding Author: Arne Søraas, PhD, Department of Microbiology, Oslo University Hospital, Pb 4950, 0424 Oslo, Norway (email@example.com).
Author Contributions: Dr Søraas had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Søraas, Bø, Kalleberg.
Acquisition, analysis, or interpretation of data: All authors.
Drafting of the manuscript: Søraas, Kalleberg.
Critical revision of the manuscript for important intellectual content: All authors.
Statistical analysis: Søraas, Støer.
Administrative, technical, or material support: Søraas, Kalleberg.
Supervision: Søraas, Ellingjord-Dale.
Conflict of Interest Disclosures: Dr Søraas reported being an employee and shareholder at Age Labs outside of the submitted work. Dr Kalleberg reported receiving grants from the Norwegian Research Council during the conduct of the study and being a shareholder at Age Labs outside of the submitted work. No other disclosures were reported.
Additional Contributions: We thank Eyvind Axelsen, PhD; Andreas Lind, MD, PhD; Roar Bævre-Jensen, MD; and Silje Bakken Jørgensen, MD, PhD for contributing to the participant recruitment in this study. We also thank Mette Istre, MSc, for her contribution to establishing the cohort. Written permissions to include these nonauthors have been obtained and no one was compensated for their work.
Additional Information: The manuscript has been published on a preprint server.
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